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- Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse–Sakati syndrome
  
  Mansoor C. Abdulla Anas M. Alazami Jemshad Alungal Jassim M. Koya Mohthash Musambil
  
  Research Note Volume 94 Issue 3 September 2015 pp 489-492
- Fulltext
  
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  Permanent link:
  https://www.ias.ac.in/article/fulltext/jgen/094/03/0489-0492
- Keywords
  
  Woodhouse–Sakati syndrome; Indian family; C2orf37 gene.
- Author Affiliations
  Mansoor C. Abdulla¹ Anas M. Alazami² Jemshad Alungal¹ Jassim M. Koya³ Mohthash Musambil⁴
  1. Department of Internal Medicine, MES Medical College, Perinthalmanna 679 338, India
  2. Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh MBC-03 PO BOX 3354, Saudi Arabia
  3. Department of Radiodiagnosis, MES Medical College, Perinthalmanna 679 338, India
  4. Medical Biotechnology Central Research Lab, MES Medical College, Perinthalmanna 679 338, India
- Dates
  
  Published
  September 2015
  Manuscript received
  23 November 2014
  Manuscript revised
  11 February 2015
  Accepted
  4 March 2015
  Unedited version published online
  9 March 2015
  Early published
  14 August 2015

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